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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Cyclohexanol, 2-methyl-5-(1-methylethenyl)-, acetate, (1R,2R,5R)-rel-

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Chemical Name: Cyclohexanol, 2-methyl-5-(1-methylethenyl)-, acetate, (1R,2R,5R)-rel-
CAS Number: 20777-49-5
Product Number: AG00I3Z4(AGN-PC-0QWLRR)
Synonyms:
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Molecular Formula:
Molecular Weight:

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Chemical Structure


(±)-Dihydrocarvyl acetate is a versatile compound that finds widespread application in chemical synthesis. Its unique molecular structure and properties make it a valuable building block for creating a variety of different compounds. One of the key roles of (±)-Dihydrocarvyl acetate in chemical synthesis is as a chiral auxiliary, allowing for the controlled formation of stereochemical centers during reactions. This compound can be used to introduce chirality into molecules and influence the outcome of reactions, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. (±)-Dihydrocarvyl acetate is known for its ability to participate in a range of reactions, including asymmetric cycloadditions, aldol reactions, and Michael additions, among others. Its application in chemical synthesis extends to the creation of complex molecules with specific stereochemical features, making it an important component in the toolkit of synthetic chemists.